A Unique Phenotype in a Patient with a Rare Triplication of the 22Q11.2 Region and New Clinical Insights of the 22Q11.2 Microduplication Syndrome: a Report of Two Cases

AuthID
 P-00G-FSE
7
Author(s)
Vaz, SO
·
Pires, R
·
Anjos, R
·
Maciel, P
·
Tipo de Documento
Article
Year published
2015
Publicado
in BMC PEDIATRICS, ISSN: 1471-2431
Volume: 15, Número: 1
Indexing
Wos®
Scopus®
Crossref®5
Google Scholar®
Publication Identifiers
SCOPUS: 2-s2.0-84939535085
Wos: WOS:000359830300001
Source Identifiers
ISSN: 1471-2431
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